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23. The Chicago variant of clinical galactosemia. Chacko CM; Wappner RS; Brandt IK; Nadler HL Hum Genet; 1977 Jul; 37(3):261-70. PubMed ID: 885545 [TBL] [Abstract][Full Text] [Related]
24. [The frequency of uridyl transferase deficiency in patients with galactose intolerance]. Fernekorn A; Fiehring C Dtsch Gesundheitsw; 1976 Dec; 31(52):2455-60. PubMed ID: 1009846 [No Abstract] [Full Text] [Related]
25. Galactose intolerance in individuals with double heterozygosity for Duarte variant and galactosemia. Schwarz HP; Zuppinger KA; Zimmerman A; Dauwalder H; Scherz R; Bier DM J Pediatr; 1982 May; 100(5):704-9. PubMed ID: 7069531 [TBL] [Abstract][Full Text] [Related]
26. The first study of galactose-1-phosphate uridyl transferase mutations in Iranian galactosemia patients. Mirzajani F; Mirfakhraie R; Nabati F; Tabatabaei NN; Talachian E; Houshmand M Clin Biochem; 2006 Jul; 39(7):697-9. PubMed ID: 16765930 [TBL] [Abstract][Full Text] [Related]
27. Evaluation of reduced activity galactose-1-phosphate uridyl transferase by combined radioisotopic assay and high-resolution isoelectric focusing. Kelley RI; Segal S J Lab Clin Med; 1989 Aug; 114(2):152-6. PubMed ID: 2546999 [TBL] [Abstract][Full Text] [Related]
28. Variants of galactose-1-phosphate uridyl transferase in the Greek populations. Thomakos A; Beutler E; Stamatoyannopoulos G Hum Genet; 1977 May; 36(3):335-9. PubMed ID: 856721 [TBL] [Abstract][Full Text] [Related]
29. Study of a family with both galactosemic and Duarte variants of galactose-1-phospho uridyl transferase. Schapira F; Gregori C; Poenaru L Biochem Med; 1974 Sep; 11(1):87-92. PubMed ID: 4415964 [No Abstract] [Full Text] [Related]
30. Frequency of Gt types in the Polish population. Hałasa J; Schlesinger D Arch Immunol Ther Exp (Warsz); 1978; 26(1-6):169-71. PubMed ID: 749766 [TBL] [Abstract][Full Text] [Related]
31. Length of the chromosomal segment marked by galactose-1-phosphate uridyl transferase and soluble aconitase and conserved since divergence of lineages leading to mouse and man. Nadeau JH Genet Res; 1988 Oct; 52(2):141-4. PubMed ID: 2850257 [No Abstract] [Full Text] [Related]
32. Molecular studies on galactose 1 phosphate uridylyl transferase from normal and mutant subjects. An immunological approach. Banroques J; Schapira F; Grégori C; Dreyfus JC Ann Hum Genet; 1983 Jul; 47(3):177-85. PubMed ID: 6311074 [TBL] [Abstract][Full Text] [Related]
33. Studies on the molecular defect in galactosemia. Tedesco TA UCLA Forum Med Sci; 1975; (18):467-77. PubMed ID: 173062 [TBL] [Abstract][Full Text] [Related]
34. Starch gel electrophoresis for galactose-1-phosphate uridylyl-transferase applied to dried filter paper blood specimens. Hammersen G; Levy HL Clin Chim Acta; 1977 Jun; 77(3):295-9. PubMed ID: 872429 [TBL] [Abstract][Full Text] [Related]
36. Interallelic complementation in hybrid cells derived from human diploid strains deficient in galactose-1-phosphate uridyl transferase activity. Nadler HL; Chacko CM; Rachmeler M Proc Natl Acad Sci U S A; 1970 Oct; 67(2):976-82. PubMed ID: 5289034 [TBL] [Abstract][Full Text] [Related]
37. Gene dosage studies supporting localization of the structural gene for galactose-1-phosphate uridyl transferase (GALT) to band p13 of chromosome 9. Shih LY; Suslak L; Rosin I; Searle BM; Desposito F Am J Med Genet; 1984 Nov; 19(3):539-43. PubMed ID: 6095663 [TBL] [Abstract][Full Text] [Related]
38. Galactose-1-phosphate uridyl transferase activity associated with age at menopause and reproductive history. Cramer DW; Harlow BL; Barbieri RL; Ng WG Fertil Steril; 1989 Apr; 51(4):609-15. PubMed ID: 2538369 [TBL] [Abstract][Full Text] [Related]